Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799939
rs1799939
RET
27 0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 0.020 1.000 2 2015 2016
dbSNP: rs1238981206
rs1238981206
ERBB2 ; MIR4728
3 0.925 0.080 17 39724828 missense variant G/A snv 4.0E-06 0.010 1.000 1 2015 2015